Asperpyridone A: An Unusual Pyridone Alkaloid Exerts Hypoglycemic Activity through the Insulin Signaling Pathway.
Yuben QiaoQianqian XuWenya FengLi TaoXiao-Nian LiJun-Jun LiuHucheng ZhuYuanyuan LuJianping WangChangxing QiYongbo XueYong-Hui ZhangPublished in: Journal of natural products (2019)
A pyridone alkaloid, asperpyridone A (1), which possesses an unusual pyrano[3,2-c]pyridine scaffold, was isolated from solid cultures of the endophytic fungus Aspergillus sp. TJ23. Its structure, including its absolute configuration, was determined using a combination of nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, quantum chemical calculations (electronic circular dichroism), and X-ray crystallography. In vitro bioassays demonstrated that asperpyridone A (1) could function as a potential hypoglycemic agent, which exhibited pronounced glucose uptake effect in liver HepG2 cells, under both normal and insulin-resistant conditions, with higher efficacy than metformin. The underlying mechanism of asperpyridone A was elucidated by analyzing the genes expressed, the Gene Ontology (GO) function enrichment, the protein interaction network, and real-time quantitative reverse transcription polymerase chain reaction, which suggested that asperpyridone A exhibits hypoglycemic activity by activating the insulin signaling pathway. Moreover, on the basis of the hypoglycemic potency, fibroblast growth factor 21 (FGF21) was determined to be a potential target for asperpyridone A.
Keyphrases
- high resolution
- signaling pathway
- type diabetes
- mass spectrometry
- magnetic resonance
- pi k akt
- glycemic control
- molecular dynamics
- genome wide
- epithelial mesenchymal transition
- induced apoptosis
- magnetic resonance imaging
- density functional theory
- genome wide identification
- human health
- risk assessment
- small molecule
- high speed
- cell proliferation
- binding protein
- capillary electrophoresis
- skeletal muscle
- electron microscopy